Apply for Safety Science Coordinator I job at Fortrea Pune. Check eligibility, experience, last date, and application process details now.
Introduction
If you are looking to build a strong career in clinical safety and pharmacovigilance, this opportunity is worth exploring. The Safety Science Coordinator I Job at Fortrea offers hands-on experience in adverse event processing, regulatory submissions, and clinical safety operations. Ideal for pharmacy and life sciences professionals, this role provides exposure to global safety systems and clinical trial environments.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Safety Science Coordinator I |
| Company Name | Fortrea |
| Location | Pune, India |
| Employment Type | Full-time |
| Department | Clinical Safety / Pharmacovigilance |
| Experience Required | Minimum 2+ Years |
| Education | B.Pharm / M.Pharm / Pharm.D / Life Sciences |
| Salary | As per company norms |
Company Overview
Fortrea is a leading global contract research organization (CRO) specializing in clinical development, patient safety, and regulatory services. The company partners with pharmaceutical, biotechnology, and medical device companies to support clinical trials and drug development worldwide. Fortrea is known for its strong focus on innovation, compliance, and high-quality clinical research services.
Job Location & Employment Type
- Location: Pune, Maharashtra, India
- Work Mode: Office-based
- Job Type: Full-time
This role requires candidates to work in a structured office environment with cross-functional teams.
Open Positions / Department Details
- Department: Clinical Safety / Patient Safety Services (PSS)
- Role Focus:
- Adverse event processing
- Clinical safety reporting
- Regulatory compliance
Key Roles & Responsibilities
As a Safety Science Coordinator I, you will be responsible for:
Safety Case Processing & Reporting
- Assisting in processing Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)
- Managing adverse event (AE) and serious adverse event (SAE) data
- Submitting safety reports to regulatory authorities and stakeholders within timelines
Data Management & Documentation
- Maintaining adverse event tracking systems and project files
- Entering safety data into clinical databases
- Managing documentation for clinical safety projects
Medical Writing & Evaluation
- Writing patient narratives for adverse event cases
- Coding adverse events using MedDRA terminology
- Supporting listedness assessment against product labels
Query Handling & Coordination
- Generating queries for missing or inconsistent safety data
- Coordinating with medical teams for data clarification
- Assisting in database reconciliation and quality checks
Compliance & Quality Management
- Working within SOPs, WIs, and Quality Management Systems
- Supporting audit readiness and regulatory compliance
- Ensuring high-quality data processing standards
Team Support & Operations
- Assisting in training junior team members
- Supporting internal and external meetings
- Maintaining effective collaboration across departments
Eligibility Criteria
Education
- B.Pharm / M.Pharm / Pharm.D
- OR Degree in:
- Nursing
- Medical Sciences
- Life Sciences
Experience
- Minimum 2+ years of experience in:
- Clinical trial safety case processing
- AE/SAE handling
- Pharmacovigilance operations
Skills Required
- Knowledge of pharmacovigilance and clinical safety processes
- Experience with safety databases and regulatory submissions
- Strong understanding of AE/SAE reporting
- Good communication and writing skills
- Attention to detail and analytical ability
- Ability to multitask and manage deadlines
- Proficiency in MS Office tools
- Strong teamwork and coordination skills
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a global CRO
- Exposure to international clinical trials and safety systems
- Career growth in pharmacovigilance and clinical safety
- Structured training and development programs
- Collaborative work environment
Selection Process
The hiring process generally includes:
- Application screening
- Technical interview (Clinical Safety / PV focus)
- HR discussion
Candidates with hands-on experience in AE/SAE processing will be preferred.
How to Apply
- Apply through the official job portal before the deadline
Important Dates
- Last Date to Apply: April 8, 2026
Why Apply for This Job?
The Safety Science Coordinator I Job at Fortrea provides an excellent platform for professionals looking to grow in pharmacovigilance and clinical safety. With exposure to global regulatory systems and clinical trials, candidates can develop strong expertise in safety reporting and compliance.
Working with a reputed CRO like Fortrea also enhances career opportunities in the pharmaceutical and biotechnology sectors, making this role highly valuable for long-term growth.
FAQs
1. What is the main responsibility of this role?
The role involves processing adverse event reports, managing safety data, and supporting regulatory submissions.
2. What qualifications are required?
Candidates need a degree in Pharmacy, Life Sciences, Nursing, or related fields.
3. What experience is needed?
At least 2 years of experience in clinical safety or pharmacovigilance is required.
4. Where is the job located?
The position is based in Pune and requires office-based work.
5. What is the last date to apply?
The last date to apply is April 8, 2026.
Conclusion
The Safety Science Coordinator I Job at Fortrea is a strong opportunity for professionals aiming to build expertise in clinical safety and pharmacovigilance. With global exposure, structured processes, and career growth potential, this role is ideal for candidates looking to advance in the CRO industry. Apply before the deadline to secure your chance.
Disclaimer
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